Sector Retinitis Pigmentosa caused by mutations of the RHO gene

被引:0
|
作者
Li, Yang [1 ]
Xu, Ke [1 ]
Xiao, Ting [1 ]
Zhang, Xiaohui [1 ]
Xie, Yue [1 ]
机构
[1] Beijing Tongren Hosp, Beijing Inst Ophthalmol, Beijing, Peoples R China
关键词
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
5422
引用
收藏
页数:2
相关论文
共 50 条
  • [21] MUTATIONS IN THE USH1C GENE ASSOCIATED WITH SECTOR RETINITIS PIGMENTOSA AND HEARING LOSS
    Saihan, Zubin
    Stabej, Polona Le Quesne
    Robson, Anthony G.
    Rangesh, Nell
    Holder, Graham E.
    Moore, Anthony T.
    Steel, Karen P.
    Luxon, Linda M.
    Bitner-Glindzicz, Maria
    Webster, Andrew R.
    RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2011, 31 (08): : 1708 - 1716
  • [22] Gene therapy With Self-complementary Recombinant Adeno-associated Virus in Models of Autosomal Dominant Retinitis Pigmentosa Caused by RHO Mutations
    Rossmiller, Brian P.
    Mao, Haoyu
    Lewin, Alfred S.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [23] Gene Therapy with Self-Complementary Recombinant Adeno-Associated Virus in Models of Autosomal Dominant Retinitis Pigmentosa Caused by RHO Mutations
    Rossmiller, Brian P.
    Mao, Haoyu
    Lewin, Alfred
    MOLECULAR THERAPY, 2014, 22 : S48 - S48
  • [24] Novel therapeutic approaches for Retinitis Pigmentosa caused by mutations in Rhodopsin
    Marigo, Valeria
    Comitato, Antonella
    La Marca, Clara
    Subramanian, Preeti
    Felline, Angelo
    Fanelli, Francesca
    Becerra, S. Patricia
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [25] Arrestin gene mutations in autosomal recessive retinitis pigmentosa
    Nakazawa, M
    Wada, Y
    Tamai, M
    ARCHIVES OF OPHTHALMOLOGY, 1998, 116 (04) : 498 - 501
  • [26] A screen for mutations of the IMPGI gene in patients with retinitis pigmentosa
    Adam, SM
    Dryja, TP
    Berson, EL
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U940 - U940
  • [27] Post-receptoral rod and cone abnormalities in retinitis pigmentosa caused by rhodopsin gene mutations
    Cideciyan, AV
    Hood, DC
    Regunath, G
    Sheffield, VC
    Stone, EM
    Nathans, J
    Jacobson, SG
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 2284 - 2284
  • [28] New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene
    Sakamoto, Kenji
    McCluskey, Michael
    Wensel, Theodore G.
    Naggert, Juergen K.
    Nishina, Patsy M.
    HUMAN MOLECULAR GENETICS, 2009, 18 (01) : 178 - 192
  • [29] Gene Therapy for Retinitis Pigmentosa Caused by MFRP Mutations: Human Phenotype and Preliminary Proof of Concept
    Dinculescu, Astra
    Estreicher, Jackie
    Zenteno, Juan C.
    Aleman, Tomas S.
    Schwartz, Sharon B.
    Huang, Wei Chieh
    Roman, Alejandro J.
    Sumaroka, Alexander
    Li, Qiuhong
    Deng, Wen-Tao
    Min, Seok-Hong
    Chiodo, Vince A.
    Neeley, Andy
    Liu, Xuan
    Shu, Xinhua
    Matias-Florentino, Margarita
    Buentello-Volante, Beatriz
    Boye, Sanford L.
    Cideciyan, Artur V.
    Hauswirth, William W.
    Jacobson, Samuel G.
    HUMAN GENE THERAPY, 2012, 23 (04) : 367 - 376
  • [30] Analysis of choriocapillaris vascular density changes in patients with retinitis pigmentosa caused by RPGR gene mutations
    Marano, Ernesto
    Gesualdo, Carlo
    Del Giudice, Antonio
    Guarino, Francesco
    Melillo, Paolo
    Rossi, Settimio
    Testa, Francesco
    Simonelli, Francesca
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2023, 64 (08)